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. 2023:2693:163-174.
doi: 10.1007/978-1-0716-3342-7_13.

Using a Modified Proximity Ligation Protocol to Study the Interaction Between Chaperones and Associated Proteins

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Using a Modified Proximity Ligation Protocol to Study the Interaction Between Chaperones and Associated Proteins

Simone Baldan et al. Methods Mol Biol. 2023.

Abstract

Molecular chaperones can interact with multiple proteins to form large networks. Understanding these interactions may shed light on the complexity of the chaperone functions. Here we developed a protocol for a modified proximity ligation-based methodology (PLA) for the detection of protein-protein interactions in order to understand how the Hsp70-Bag3 complex interacts with components of the Hippo signaling pathway. These experiments helped to elucidate the mechanisms of transmission of the proteotoxic stress signal to the Hippo pathway. The modified PLA technology has many advantages compared to co-immunoprecipitation protocols. It has higher sensitivity, is quantitative, and can be done in a 96-well format.

Keywords: Bag3; Hippo pathway; Hsp70; LATS1/2; Protein complex; Proximity ligation assay; Yap.

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References

    1. Hartl FU, Bracher A, Hayer-Hartl M (2011) Molecular chaperones in protein folding and proteostasis. Nature 475:324–332 - DOI - PubMed
    1. Chaperone machines for protein folding, unfolding and disaggregation | Nature Reviews Molecular Cell Biology, https://www.nature.com/articles/nrm3658
    1. Morán Luengo T, Mayer MP, Rüdiger SGD (2019) The Hsp70-Hsp90 chaperone cascade in protein folding. Trends Cell Biol 29:164–177 - DOI - PubMed
    1. Rosenzweig R, Nillegoda NB, Mayer MP et al (2019) The Hsp70 chaperone network. Nat Rev Mol Cell Biol 20:665–680 - DOI - PubMed
    1. Kampinga HH, Craig EA (2010) The HSP70 chaperone machinery: J proteins as drivers of functional specificity. Nat Rev Mol Cell Biol 11:579–592 - DOI - PubMed - PMC

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